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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243571Generated: October 30, 2026

Trifluoroacetic acid → HCID 11663885, compound

https://huagongshe.com/reaction/2243571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58608133HCID 58608133—
SolventDichloromethaneHCID 6344—
ProductHCID 11663885HCID 11663885—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 4-(2-{2-[4-(2-diisopropylamino-ethoxy)-phenyl]-3-phenyl-furo[2,3-b]pyridin-4-ylamino}-ethyl)-piperazine-1-carboxylic acid tert-butyl ester 10a (0.075 g, 0.117 mmol) in dichloromethane (2.0 mL) was cooled to 0° C. Trifluoroacetic acid (1.0 mL) was added and the solution stirred under a nitrogen atmosphere at 0° C. and was allowed to warm to room temperature over 2 h. The reaction mixture was concentrated and the residue was partitioned between dichloromethane and saturated aqueous sodium bicarbonate solution. The organic phase was separated and washed with saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate, filtered and concentrated to afford {2-[4-(2-diisopropylamino-ethoxy)-phenyl]-3-phenyl-furo[2,3-b]pyridin-4-yl}-(2-piperazin-1-yl-ethyl)-amine 10b as an off-white solid. MS (MH+) 542.3; Calculated 541 for C33H43N5O2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674907B2
Source datasetuspto-grants-2010_03
ORD IDord-79c72c6437794c7088557a73ffaa99c5
Source noteuspto-grants-2010_03